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Dive into the research topics where Montserrat Fernandez-Rivas is active.

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Featured researches published by Montserrat Fernandez-Rivas.


The Journal of Allergy and Clinical Immunology | 2003

Clinically relevant peach allergy is related to peach lipid transfer protein, Pru p 3, in the spanish population

Montserrat Fernandez-Rivas; E. González-Mancebo; Rosa Rodriguez-Perez; Cristina Benito; Rosa Sánchez-Monge; Gabriel Salcedo; M. Dolores Alonso; A. Rosado; M.A. Tejedor; A. Conception Vila; M. Luisa Casas

BACKGROUND Sensitization to peach and related Rosaceae fruits without clinical expression is commonly observed as the result of the extensive cross-reactivity of IgE antibodies directed toward lipid transfer proteins (LTPs), Bet v 1 homologues, profilins, and carbohydrate determinants. OBJECTIVE We aimed to study whether there are any clinical or immunologic differences between patients allergic to peach and those who have a current clinically irrelevant sensitization to this fruit. METHODS One hundred subjects with adverse reactions to peach were evaluated by medical history, skin prick tests with fresh peach and purified peach LTP (Pru p 3), and specific IgE determinations to peach, rBet v 1, and rBet v 2 (birch profilin). Clinical reactivity to peach was established by double-blind, placebo-controlled food challenges. The clinical characteristics and the in vivo and in vitro tests were compared between allergic and nonallergic patients. RESULTS Peach allergy was confirmed in 76 patients and ruled out in 16; 2 patients dropped out, and the study was not conclusive in 6 individuals (placebo reactors). Pollen allergy was found in 76% of the allergic patients and in 100% of the nonallergic patients. Positive responses to Pru p 3, rBet v 1, and rBet v 2 were observed in 62%, 7%, and 34% of patients allergic to peach, respectively. The sensitization rate to Pru p 3 was significantly higher among subjects allergic than nonallergic to peach (62% vs 31%, P =.02). IgE responses to rBet v 2 were more frequent among subjects allergic to pollen, but no difference was observed in the presence or absence of peach allergy. CONCLUSIONS Pru p 3 is the major allergen of peach in our population, and the IgE response to this allergen is related to the clinical expression of peach allergy. Sensitization to profilin is observed in those patients with an associated pollen allergy but does not appear to be related to the clinical reactivity to peach.


Clinical & Experimental Allergy | 2000

Lipid‐transfer proteins as potential plant panallergens: cross‐reactivity among proteins of Artemisia pollen, Castanea nut and Rosaceae fruits, with different IgE‐binding capacities

Araceli Díaz-Perales; M. Lombardero; Rosa Sánchez-Monge; F. J. García‐Sellés; M. Pernas; Montserrat Fernandez-Rivas; Domingo Barber; Gabriel Salcedo

Lipid‐transfer proteins (LTPs), but not Bet v 1 homologues, have been identified as major allergens of apple and peach in the Rosaceae fruit‐allergic population in the Mediterranean area. Many of these patients show cosensitization to mugwort pollen. LTPs have an ubiquitous distribution in tissues of many plant species, and have been proposed as a novel type of plant panallergens.


The Journal of Allergy and Clinical Immunology | 1997

Allergy to Rosaceae fruits without related pollinosis

Montserrat Fernandez-Rivas; Ronald van Ree; Manuela Cuevas

BACKGROUND Rosaceae fruit allergy is frequently associated with birch pollinosis in Central and Northern Europe and with grass pollen allergy in Central Spain. The main cross-reactive structures involved for birch pollinosis are Bet v 1 and profilin, and for grass pollinosis they are profilin and carbohydrate determinants. Rosaceae fruit allergy can occasionally be observed in patients without pollinosis. OBJECTIVE We investigated the clinical presentation and the allergens involved in allergy to Rosaceae fruit without pollinosis. METHODS Eleven patients from Central Spain allergic to apples, peaches, and/or pears but not to pollens were compared with 22 control subjects with combined grass pollen and fruit allergy. Skin prick tests and RASTs to apple, peach, and pear were performed. Cross-allergenicity was studied by RAST inhibition. Bet v 1 was tested with an indirect RAST, and profilin was tested in skin prick tests, histamine release, and RAST. RESULTS Rosaceae fruit allergy without pollinosis is severe with 82% of patients reporting systemic symptoms, mainly anaphylaxis (73%), whereas oral symptoms are less frequent (64%). Anaphylactic shock was observed in 36% of patients. The fruit allergens involved showed cross-reactivity among Rosaceae species but were not related to profilin or Bet v 1. Ninety-one percent of patients with combined grass pollinosis and fruit allergy reported oral allergy, 45% reported systemic symptoms, 18% reported anaphylaxis, and 9% reported anaphylactic shock. CONCLUSION Allergy to Rosaceae fruits in patients without a related pollen allergy is a severe clinical entity. Profilin- and Bet v 1-related structures are not involved in Rosaceae fruit allergy without pollinosis.


Allergy | 2009

Randomized double-blind, placebo-controlled trial of sublingual immunotherapy with a Pru p 3 quantified peach extract.

Montserrat Fernandez-Rivas; S. Garrido Fernández; J. A. Nadal; M. D. Alonso Díaz de Durana; Blanca E. García; E. González-Mancebo; Santiago Martín; Domingo Barber; P. Rico; Ana Isabel Tabar

Background:  Peach allergy is highly prevalent in the Mediterranean area; it is persistent and potentially severe, and therefore a prime target for immunotherapy. We aimed to study the efficacy and safety of sublingual immunotherapy (SLIT) with a peach extract quantified in mass units for Pru p 3, the peach lipid transfer protein.


Pediatric Allergy and Immunology | 2016

EAACI Molecular Allergology User's Guide

Paolo Maria Matricardi; Jörg Kleine-Tebbe; Hans Jürgen Hoffmann; Rudolf Valenta; Christiane Hilger; Stephanie Hofmaier; Rob C. Aalberse; Ioana Agache; Riccardo Asero; Barbara K. Ballmer-Weber; D. Barber; Kirsten Beyer; T. Biedermann; Maria Beatrice Bilò; S. Blank; Barbara Bohle; P. P. Bosshard; H. Breiteneder; Helen A. Brough; Luis Caraballo; J. C. Caubet; Janet M. Davies; Nikolaos Douladiris; Philippe Eigenmann; Montserrat Fernandez-Rivas; Fatima Ferreira; Gabriele Gadermaier; M. Glatz; R. G. Hamilton; Thomas Hawranek

The availability of allergen molecules (‘components’) from several protein families has advanced our understanding of immunoglobulin E (IgE)‐mediated responses and enabled ‘component‐resolved diagnosis’ (CRD). The European Academy of Allergy and Clinical Immunology (EAACI) Molecular Allergology Users Guide (MAUG) provides comprehensive information on important allergens and describes the diagnostic options using CRD. Part A of the EAACI MAUG introduces allergen molecules, families, composition of extracts, databases, and diagnostic IgE, skin, and basophil tests. Singleplex and multiplex IgE assays with components improve both sensitivity for low‐abundance allergens and analytical specificity; IgE to individual allergens can yield information on clinical risks and distinguish cross‐reactivity from true primary sensitization. Part B discusses the clinical and molecular aspects of IgE‐mediated allergies to foods (including nuts, seeds, legumes, fruits, vegetables, cereal grains, milk, egg, meat, fish, and shellfish), inhalants (pollen, mold spores, mites, and animal dander), and Hymenoptera venom. Diagnostic algorithms and short case histories provide useful information for the clinical workup of allergic individuals targeted for CRD. Part C covers protein families containing ubiquitous, highly cross‐reactive panallergens from plant (lipid transfer proteins, polcalcins, PR‐10, profilins) and animal sources (lipocalins, parvalbumins, serum albumins, tropomyosins) and explains their diagnostic and clinical utility. Part D lists 100 important allergen molecules. In conclusion, IgE‐mediated reactions and allergic diseases, including allergic rhinoconjunctivitis, asthma, food reactions, and insect sting reactions, are discussed from a novel molecular perspective. The EAACI MAUG documents the rapid progression of molecular allergology from basic research to its integration into clinical practice, a quantum leap in the management of allergic patients.


Allergy | 2013

The epidemiology of anaphylaxis in Europe: a systematic review

Sukhmeet S Panesar; Sundas Javad; D. de Silva; Bright I. Nwaru; L. Hickstein; Antonella Muraro; Graham Roberts; Margitta Worm; M.B. Bilò; Victoria Cardona; Anthony Dubois; A. Dunn Galvin; Philippe Eigenmann; Montserrat Fernandez-Rivas; Susanne Halken; Gideon Lack; Bodo Niggemann; Alexandra F. Santos; B. J. Vlieg-Boerstra; Z.Q. Zolkipli; Aziz Sheikh

Anaphylaxis is an acute, potentially fatal, multi‐organ system, allergic reaction caused by the release of chemical mediators from mast cells and basophils. Uncertainty exists around epidemiological measures of incidence and prevalence, risk factors, risk of recurrence, and death due to anaphylaxis. This systematic review aimed to (1) understand and describe the epidemiology of anaphylaxis and (2) describe how these characteristics vary by person, place, and time.


The Journal of Allergy and Clinical Immunology | 2016

Anaphylaxis in children and adolescents: The European Anaphylaxis Registry.

Linus Grabenhenrich; Sabine Dölle; Anne Moneret-Vautrin; Alice Köhli; Lars Lange; Thomas Spindler; Franziska Ruëff; Katja Nemat; Ioana Maris; Eirini Roumpedaki; Kathrin Scherer; Hagen Ott; Thomas Reese; Tihomir Mustakov; Roland Lang; Montserrat Fernandez-Rivas; Marek L. Kowalski; Maria Beatrice Bilò; Jonathan O'b Hourihane; Nikolaos G. Papadopoulos; Kirsten Beyer; Antonella Muraro; Margitta Worm

BACKGROUND Anaphylaxis in children and adolescents is a potentially life-threatening condition. Its heterogeneous clinical presentation and sudden occurrence in virtually any setting without warning have impeded a comprehensive description. OBJECTIVE We sought to characterize severe allergic reactions in terms of elicitors, symptoms, emergency treatment, and long-term management in European children and adolescents. METHODS The European Anaphylaxis Registry recorded details of anaphylaxis after referral for in-depth diagnosis and counseling to 1 of 90 tertiary allergy centers in 10 European countries, aiming to oversample the most severe reactions. Data were retrieved from medical records by using a multilanguage online form. RESULTS Between July 2007 and March 2015, anaphylaxis was identified in 1970 patients younger than 18 years. Most incidents occurred in private homes (46%) and outdoors (19%). One third of the patients had experienced anaphylaxis previously. Food items were the most frequent trigger (66%), followed by insect venom (19%). Cows milk and hens egg were prevalent elicitors in the first 2 years, hazelnut and cashew in preschool-aged children, and peanut at all ages. There was a continuous shift from food- to insect venom- and drug-induced anaphylaxis up to age 10 years, and there were few changes thereafter. Vomiting and cough were prevalent symptoms in the first decade of life, and subjective symptoms (nausea, throat tightness, and dizziness) were prevalent later in life. Thirty percent of cases were lay treated, of which 10% were treated with an epinephrine autoinjector. The fraction of intramuscular epinephrine in professional emergency treatment increased from 12% in 2011 to 25% in 2014. Twenty-six (1.3%) patients were either admitted to the intensive care unit or had grade IV/fatal reactions. CONCLUSIONS The European Anaphylaxis Registry confirmed food as the major elicitor of anaphylaxis in children, specifically hens egg, cows milk, and nuts. Reactions to insect venom were seen more in young adulthood. Intensive care unit admissions and grade IV/fatal reactions were rare. The registry will serve as a systematic foundation for a continuous description of this multiform condition.


The Journal of Allergy and Clinical Immunology | 2008

The European Union CREATE Project: A model for international standardization of allergy diagnostics and vaccines

Martin D. Chapman; Fatima Ferreira; Mayte Villalba; Oliver Cromwell; Donna Bryan; Wolf-Meinhard Becker; Montserrat Fernandez-Rivas; Stephen R. Durham; Stefan Vieths; Ronald van Ree

Allergen measurements are used extensively in the formulation of allergy diagnostics and vaccines, yet no purified international allergen standards are available for calibration purposes. The aims of the European Union CREATE project were to develop international standards with verifiable allergen content. Purified natural and recombinant allergens were analyzed by means of SDS-PAGE, mass spectrometry, circular dichroism spectra, and small-angle x-ray scattering. IgE reactivity was assessed by means of direct RAST, RAST inhibition, immunoblotting, and basophil histamine release with sera from 961 allergic patients. Three recombinant allergens, rBet v 1, rPhl p 5a, and rDer p 2, were structurally indistinguishable from their natural counterparts and showed excellent IgE reactivity suitable for use as certified reference materials. A second tier of allergens (rPhl p 5b, rOle e1, rDer p 1, rDer f 1, and rDer f 2) was identified that could provide suitable candidates for certified reference materials with minor improvements to the recombinant proteins. Only rPhl p 1 was considered unsuitable as a reference material. Quantitative ELISAs were identified that accurately measured each allergen, except for rPhl p 1. The CREATE project has provided a major step forward in allergen standardization and provides a model for the development of a comprehensive panel of international reference preparations that will harmonize allergen measurements worldwide.


Allergy | 2014

First European data from the network of severe allergic reactions (NORA)

Margitta Worm; Anne Moneret-Vautrin; Kathrin Scherer; Roland Lang; Montserrat Fernandez-Rivas; Victoria Cardona; M. L. Kowalski; Marek Jutel; I. Poziomkowska-Gesicka; Nikolaos G. Papadopoulos; Kirsten Beyer; Tihomir Mustakov; George Christoff; Maria Beatrice Bilò; Antonella Muraro; Jonathan O'b Hourihane; Linus Grabenhenrich

Occurrence, elicitors and treatment of severe allergic reactions are recognized and reported differently between countries. We aimed to collect standardized data throughout Europe on anaphylaxis referred for diagnosis and counselling.


The Journal of Allergy and Clinical Immunology | 2008

Safety and effectiveness of immunotherapy in patients with indolent systemic mastocytosis presenting with Hymenoptera venom anaphylaxis.

David González de Olano; Iván Álvarez-Twose; María I. Esteban-López; Laura Sánchez-Muñoz; María D. Alonso Díaz de Durana; Arantza Vega; Andrés C. García-Montero; E. González-Mancebo; Teresa Belver; María D. Herrero-Gil; Montserrat Fernandez-Rivas; Alberto Orfao; Belén de la Hoz; Mariana Castells; Luis Escribano

BACKGROUND Anaphylaxis after Hymenoptera sting has been described in patients with mastocytosis. Venom immunotherapy (VIT) is a safe and effective way to treat patients with Hymenoptera anaphylaxis, but few studies have addressed its usefulness in patients with systemic mastocytosis. OBJECTIVE To study the effectiveness and safety of VIT in patients with systemic mastocytosis having anaphylaxis after Hymenoptera sting. METHODS A total of 21 mastocytosis patients-4 women (19%) and 17 men (81%) with a median age of 50 years (range, 29-74 years)-with Hymenoptera sting anaphylaxis who were treated with VIT and followed for a median of 52 months (range, 2-250 months) were studied. RESULTS In 18 of 21 patients-16 of them lacking skin involvement-anaphylaxis was the presenting symptom. Six patients (29%) experienced adverse reactions during VIT, 3 during initiation and 3 during maintenance. Twelve patients (57%) were resting while undergoing VIT; 9 (75%) presented local reactions and 3 (25%) systemic reactions, 1 of which required intubation. The Hymenoptera specific IgE decreased from 4.15 kU/L (range, 0.44-100 kU/L) before immunotherapy to 1.2 kU/L (range, 0.34-69.4 kU/L) after 4 years (P < .003). CONCLUSION Venom immunotherapy is effective to treat IgE-mediated Hymenoptera anaphylaxis in patients with mastocytosis. Its use is recommended despite a relatively high risk of adverse reactions during the build-up phase because it provides protection from anaphylaxis in around 3/4 of the patients.

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R. van Ree

University of Amsterdam

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Michael Clausen

Boston Children's Hospital

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